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Journal ArticleDOI

Stereoselective Intramolecular Aminocarbonylation of 3-Hydroxypent-4-enylamides Catalyzed by Palladium

TLDR
The urethanes and to-samides of 3-hydroxypent-4-enylamine and its C1  C4 substituted derivatives undergo the palladium catalyzed intramolecular aminocarbonylation (0.1 equiv of PdCl2, 3.0 equivaliv of NaOAc in acetic acid under ca. 1 atm of CO).
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This article is published in Tetrahedron Letters.The article was published on 1985-01-01. It has received 54 citations till now. The article focuses on the topics: Intramolecular reaction & Palladium.

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Palladium(II)-Catalyzed Alkene Functionalization via Nucleopalladation: Stereochemical Pathways and Enantioselective Catalytic Applications

TL;DR: Enantioselective PdII-catalyzed functionalization of alkenes has experienced considerably less success than have many other classes of enantiOSElective transformations, despite the extensive history of the Wacker process and related oxidation reactions.
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Palladium‐Catalyzed Oxidative Carbonylation Reactions

TL;DR: The oxidative addition step could be potentially avoided in oxidative reactions, but only few reviews exist in this area, and the recent development in the oxidative carbonylation reactions are summarized.
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